10,000 results · 140ms · Sources: EU EUDAMED, US FDA

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FDA UDI
TELEFLEX INCORPORATED·10801902194050·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Rotato...

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FDA UDI
TELEFLEX INCORPORATED·10801902121254·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·10801902194098·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·10801902196610·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·00801902013101·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·00801902013170·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·00801902026200·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·10801902121308·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·20801902156758·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·20801902156741·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·10801902194104·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·10801902121292·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·00801902025319·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·10801902196603·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

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FDA UDI
TELEFLEX INCORPORATED·10801902121315·Arrow-Trerotola(TM) Over-The-Wire PTD(R) Kit (P...

ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD

FDA 510(k)
FDA Class 2 ·Cardiovascular

MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD

FDA 510(k)
FDA Class 2 ·Anesthesiology

Chemotherapy Gloves

FDA registration
3A GLOVE SDN. BHD.·3 products·🇲🇾 Malaysia

Patient Examination Gloves

FDA registration
3A GLOVE SDN. BHD.·1 product·🇲🇾 Malaysia

Powder Free Nitrile Examination Glove, Non-sterile, Tested for Use with Chemotherapy Drugs, and the Opioid Fentanyl citrate, simulated Gastric Acid, and Fentanyl in Gastric Acid (Blue)

FDA 510(k)
FDA Class 1 ·General Hospital